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Find Clinical Drug Pipeline Developments & Deals by IAMA Therapeutics
IAMA-6 is an orally administered small molecule therapeutic designed to directly target and inhibit NKCC1-associated neuronal hyperexcitability. It is under phase 1 clinical development for the treatment of Autism & Epilepsy.
IAMA-6 is an orally administered small molecule therapeutic targeting NKCC1. Its clinical trial application is approved after the preclinical studies for the treatment of autism and epilepsy.
Evotec will provide IAMA with preclinical and clinical services to support the anticipated Phase 1 clinical trial to investigate IAMA's lead program IAMA-6, a small molecule therapeutic targeting NKCC1 for the treatment of autism and epilepsy.
The collaboration aims to investigate the efficacy of selective chloride modulator, IAMA-6, in reducing neuronal excitability and hippocampal activity in human tissue with epilepsies and neurodevelopmental disorders, including Dravet syndrome, FCD, and Rett syndrome.
PsychoGenics will evaluate the anti-seizure efficacy of first-in-class selective-NKCC1 inhibitors, which restore the physiological hyperpolarizing and inhibitory GABAergic transmission in a preclinical model of Dravet syndrome.
Under the agreement, PsychoGenics will evaluate the preclinical anti-seizure efficacy of first-in-class selective-NKCC1 inhibitors, which aims to reduce intracellular chloride concentration and restore the physiological hyperpolarizing and inhibitory GABAergic transmission.
IAMA-6 is a first-in-class selective-NKCC1 inhibitor that modulates the intracellular chloride, reducing the depolarizing strength of GABAA receptors to the levels required to restore the inhibitory transmission.
IAMA-6 is a preclinical stage, a first-in-class selective-NKCC1 inhibitor that modulates the intracellular chloride, reducing the depolarizing strength of GABAA receptors to the levels required to restore the inhibitory transmission.
Under the collaboration with the IIT-Istituto Italiano di Tecnologia (Italian Institute of Technology), they will design and profile new classes of compounds targeting cation cotransporters in the CNS area.